This report is based solely on device analysis.No information to suggest a device related adverse event or product problem was received.If additional relevant information is received, a supplemental report will be submitted.Product event summary: during manufacturer's analysis the radiofrequency programmer head failed uplink tests and therefore its cable was replaced, and it was further noted that its label was missing its backing and the label was replaced as well.Concomitant medical products: product id: 229047, software analyzer.(b)(4).
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